Liquid hydrocarbon-based copolymers bearing two cyclocarbonate ester end groups

ABSTRACT

1) Hydrocarbon-based copolymer comprising two end groups preceded by an ester function and chosen from a 2-oxo-1,3-dioxolan-4-yl (or cyclocarbonate), a dithiocyclocarbonate, an exo-vinylene cyclocarbonate and a 2-oxo-1,3-dioxolen-4-yl, the main chain of which comprises units (I) and (II)in which R0 is notably a methyl radical;and the number-average molecular mass Mn of which is between 400 and 100 000 g/mol.2) Process for preparing said copolymer, comprising:(i) a step of heating a statistical bipolymer A chosen from a poly(butadiene-isoprene), a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and then(ii) a step of heating the product formed, in the presence of a chain-transfer agent.3) Use as adhesive, as a mixture with an amine compound comprising at least two amine groups.

The present invention relates to hydrocarbon-based polymers comprisingtwo end groups of cyclocarbonate or similar type, to the process forpreparing them and to their use in the manufacture of coating, mastic oradhesive compositions.

It is known practice to use polyurethanes to manufacture variouscoating, mastic or adhesive compositions.

These compositions may be in the form of one-component or two-componentcompositions. In the latter case, the reagents required for thesynthesis of the polyurethane are stored separately, optionally in thepresence of other ingredients (additives), and are intended to be mixedbefore use of the composition, to synthesize the polyurethane at thelast moment.

Polyurethanes are conventionally synthesized by reaction of adiisocyanate with a diol.

However, diisocyanates are toxic compounds per se and are generallyobtained from phosgene, which is itself very toxic by inhalation or bycontact. The manufacturing process used industrially generally involvesthe reaction of an amine with an excess of phosgene to form anisocyanate.

Furthermore, polyisocyanates are compounds that are highly sensitive inthe presence of atmospheric moisture and require that appropriatemeasures be taken to avoid their premature crosslinking, and thus theirloss of reactivity, during their handling and storage (anhydrousconditions).

The search for alternatives to the synthesis of polyurethanes withoutusing isocyanate (or NIPU for Non-Isocyanate PolyUrethane) thusrepresents a major challenge.

This search has formed the subject of numerous studies. The approachesmost widely studied concern the use of polymers that are capable ofreacting with amines or amine oligomers to form polyurethanes orderivatives that are structurally close to polyurethanes, such aspoly(thio)urethanes, which will be generically denoted in the presentapplication by the term “polymers of polyurethane type”.

Patent application WO 2014/091173 describes hydrocarbon-based polymerscomprising two end groups bearing a 2-oxo-1,3-dioxolan-4-yl (also knownas cyclocarbonate) end group which may be obtained by ring-openingmetathesis polymerization starting from a cycloolefin, and in thepresence of a chain-transfer agent and of a metathesis catalyst.

These polymers can subsequently react with a (poly)amine to formpolymers of polyurethane type, without employing isocyanate, and whichcan advantageously be used to formulate coating, mastic or adhesivecompositions. However, this reaction is relatively lengthy and remainsto be improved.

Patent application WO 2016/162627 also describes hydrocarbon-basedpolymers comprising two end groups bearing an exo-vinylenecyclocarbonate end group which may also be obtained by ring-openingmetathesis polymerization starting from a cycloolefin, and in thepresence of a chain-transfer agent and of a metathesis catalyst.

Patent application WO 2016/185106 describes hydrocarbon-based polymerscomprising two end groups bearing a dithiocyclocarbonate (or2-thione-1,3-oxathiolan-4-yl) end group which may also be obtained byring-opening metathesis polymerization starting from a cycloolefin, andin the presence of a chain-transfer agent and of a metathesis catalyst.The latter polymers can subsequently react with a (poly)amine to formisocyanate-free poly(thio)urethanes, which may also be used to formulatecoating, mastic or adhesive compositions.

Thus, for use as a two-component adhesive, the hydrocarbon-based polymeras described in these references and the amine compound, used as curingagent, are each included in a component of a two-component compositionwhich is made available to the user. Said user thus, just at the time ofuse of the adhesive, mixes these two components, optionally under hotconditions, so as to obtain a liquid adhesive composition. Thiscomposition is applied to at least one of two faces belonging to twosubstrates to be assembled, which are placed in contact to bring abouttheir assembly.

The progress of the reaction between said hydrocarbon-based polymer andthe amine compound leads to the formation of a cohesive adhesive sealwhich ensures the solidity of the assembly of these two substrates. Thisadhesive seal thus consists mainly of the product of said reaction, andconsequently of a polyurethane or of a poly(thio)urethane, depending onthe case.

However, it may be necessary to use the hydrocarbon-based polymer asdescribed in these references in the form of a composition comprisingother constituents, for instance tackifying resins, plasticizers,adhesion promoters, one or more additives with a reinforcing effect, forinstance a mineral filler, or else one or more additives aimed atimproving the curing time (i.e. the time at the end of which thecrosslinking can be regarded as complete) or other characteristics, suchas the rheology or the mechanical performance (elongation, modulus,etc.).

The hydrocarbon-based polymers described in the prior art referencesmentioned previously may be liquid, but they are then obtained fromsubstituted cycloolefins that are difficult to access industrially asstarting materials.

Said hydrocarbon-based polymers described are more generally solid, andmust thus be applied while hot for the purpose of mixing them with thecuring agent.

However, it is more convenient for the adhesives and/or mastics industryto have available compositions which can be applied at room temperatureby the end user and which can also be manufactured industrially, also atroom temperature, by simple mixing of the hydrocarbon-based polymer andof the additional constituents mentioned above.

It is thus particularly advantageous to have available, for thispurpose, hydrocarbon-based polymers bearing end groups of cyclocarbonateor similar type, which are themselves liquid at room temperature.

The aim of the present invention is to propose novel polymers bearingtwo end groups of cyclocarbonate or similar type, which overcome thesedrawbacks.

Another aim of the present invention is to propose polymers that areliquid at room temperature, which can lead, after mixing with a curingagent, to the formation of an adhesive seal having improved mechanicalproperties.

Another aim of the present invention is to propose polymers that areliquid at room temperature, the synthesis of which does not involveisocyanates, and which are capable of reacting with a poly(amine) in ashort time, to form polymers of polyurethane type.

Another aim of the present invention is to propose liquid polymersbearing end groups of cyclocarbonate or similar type, which are notablyof lower viscosity at room temperature, and which may also bemanufactured via a process which uses starting materials that are widelyindustrially available.

Another aim of the present invention is to propose such polymers, whichcan also be manufactured industrially via a process whose exothermicityis easier to control.

It has now been found that these aims may be achieved, in total or inpart, by means of the hydrocarbon-based polymer described below.

Thus, the present invention relates to a hydrocarbon-based copolymer Pcomprising two end groups F¹ and F² of cyclocarbonate and similar type,having the respective formulae:

in which:

-   -   g and d, which may be identical or different, represent an        integer equal to 0, 1, 2 or 3; and    -   G and D are two monovalent radicals such that the pair (G, D) is        chosen from pairs as follows:        -   (G1, D1) of formulae:

in which A¹ is an alkylene group comprising from 1 to 9 carbon atoms;

-   -   (G2, D2) of formulae:

in which A² is an alkylene group comprising from 1 to 9 carbon atoms;

-   -   (G3, D3) of formulae:

in which:

-   -   A³ is an alkylene group comprising from 1 to 9 carbon atoms;    -   A⁴, A⁵ and A⁶, which may be identical or different, each        represent a hydrogen atom, a linear or branched alkyl radical        comprising from 1 to 6 carbon atoms, a cycloalkyl radical        comprising 5 or 6 carbon atoms, a phenyl radical or an        alkylphenyl group, the alkyl chain of which comprises from 1 to        4 carbon atoms;        -   (G4, D4) of respective formulae:

in which:

-   -   A⁸ represents a hydrogen atom or a linear or branched alkyl        radical comprising from 1 to 9 carbon atoms,    -   A⁷ is an alkylene group comprising from 1 to 9 carbon atoms or a        divalent radical comprising from 1 to 20 carbon atoms and which        may be linear or branched, cyclic or heterocyclic with one or        more heteroatoms chosen from oxygen and sulfur;        -   (G5, D5) of respective formulae:

in which:

-   -   A⁹ and A¹⁰, which may be identical or different, each represent        a hydrogen atom, a linear or branched alkyl radical comprising        from 1 to 6 carbon atoms, a cycloalkyl radical comprising 5 or 6        carbon atoms, a phenyl radical or an alkylphenyl group, the        alkyl chain of which comprises from 1 to 4 carbon atoms;    -   A⁹ and A¹⁰ also possibly being bonded together to form a group        —(CH₂—)_(q)— in which q is an integer ranging from 3 to 5;        characterized in that the main chain of said copolymer P        comprises:    -   a unit (I) of formula (I) repeated p times, p being an integer        other than 0:

-   -   a unit (II) of formula (II) repeated n times, n being an integer        other than 0:

in which R⁰ represents a methyl radical or one of the three radicalshaving the following formula:

-   -   and, optionally, a unit (III) of formula (III) repeated m times,        m being an integer greater than or equal to 0:

in which:

-   -   R¹, R², R³ and R⁴, which may be identical or different,        represent:        -   a hydrogen or halogen atom; or        -   a radical comprising from 1 to 22 carbon atoms which is            chosen from alkyl, alkenyl, alkoxycarbonyl, al            kenyloxycarbonyl, alkylcarbonyloxy, alkenylcarbonyloxy and            alkylcarbonyloxyalkyl, the hydrocarbon-based chain of said            radical possibly being optionally interrupted with at least            one oxygen atom or one sulfur atom; in addition:        -   at least one of the groups R¹ to R⁴ can form, with at least            one other of the groups R¹ to R⁴ and with the carbon atom or            atoms to which said groups are linked, a 3- to 10-membered,            optionally substituted, saturated or unsaturated            hydrocarbon-based ring or heterocycle; and        -   at least one of the pairs (R¹, R²) and (R³, R⁴) can form,            with the carbon atom to which said pair is linked, a group            of two carbon atoms linked by a double bond: C═C, the other            carbon atom of which bears two substituents chosen from a            hydrogen atom and a C₁-C₄ alkyl radical; and        -   the carbon atom bearing one of the groups of the pair (R¹,            R²) may be linked to the carbon atom bearing one of the            groups of the pair (R³, R⁴) by a double bond, it being            understood that, in accordance with the valency rules, only            one of the groups of each of these two pairs is then            present;    -   R⁵ represents:        -   an oxygen or sulfur atom, or        -   a divalent radical —CH₂—, —C(═O)— or —NR⁶— in which R⁶ is an            alkyl or alkenyl radical comprising from 1 to 22 carbon            atoms;            it also being pointed out that:            the bond            represents a single bond or a double bond;            F¹ and F² are each linked to one of the two ends of the main            chain and to a unit (I); and            n, p and m are such that the number-average molecular mass            Mn of the copolymer P is within a range extending from 400            to 100 000 g/mol and its polydispersity index is within a            range extending from 1.5 to 3.0.

The various groups, radicals and letters which are included in formulaeF¹ and F² and in the definition of the main chain of the copolymer Pretain the same meaning throughout the present text, unless otherwiseindicated.

The units (I), (II) and, optionally, (Ill) are divalent radicals thatare randomly distributed in the main chain of the copolymer P, with theexception of two units (I) which are directly connected to F¹ and F².The copolymer P is thus a statistical copolymer.

The main chain of the copolymer P thus comprises two or three repeatingunits:

-   -   a first repeating unit (I) repeated p times of formula (I),    -   a second repeating unit (II) repeated n times of formula (II),        and    -   a third repeating unit (III) repeated m times of formula (III),        which is optional;        such that the copolymer P may be a bipolymer (presence of the        two repeating units (I) and (II)) or a terpolymer (presence of        the three repeating units (I), (II) and (III)).

As is apparent above, the end groups F¹ and F² are generally symmetricalrelative to the main chain, i.e. they correspond substantially, with theexception of the indices g and d.

The term “heterocycle” means a hydrocarbon-based ring which may comprisean atom other than carbon in the chain of the ring, for instance oxygen,sulfur or nitrogen atoms.

The term “end group” means a group located at one of the two ends of themain chain of the polymer.

The term “copolymer” means a polymer derived from the copolymerizationof at least two comonomers, i.e. of two chemically different monomers.The main chain of a copolymer comprises at least two chemicallydifferent repeating units.

The term “terpolymer” means a copolymer derived from thecopolymerization of three comonomers, and the main chain of whichessentially consists of three different repeating units.

The term “bipolymer” denotes a copolymer derived from thecopolymerization of two comonomers, and the main chain of whichessentially consists of two different repeating units.

The polydispersity index (also known as the PDI) is defined as the ratioMw/Mn, i.e. the ratio of the weight-average molecular mass to thenumber-average molecular mass of the polymer.

In the present text, the two average molecular masses Mn and Mw aremeasured by size exclusion chromatography (or SEC), which is alsodenoted by the term “gel permeation chromatography” (or GPC). Thecalibration performed is usually a PEG (PolyEthylene Glycol) or PS(PolyStyrene), preferably PS, calibration.

The copolymer P according to the invention is particularly homogeneousand heat-stable and advantageously liquid at room temperature. It isadvantageously, at room temperature, in the form of a viscous liquidwhose Brookfield viscosity at 23° C. is between 1 mPa·s and 150 Pa·s,preferably between 1 and 50 Pa·s.

It can react with a primary and/or secondary polyamine, in apolyaddition reaction, at a temperature of less than or equal to 80° C.and even at room temperature, to form, after a reaction time that isadvantageously short, a polymer of polyurethane type which canconstitute an adhesive seal.

The adhesive seal thus formed has high cohesive values, in particular ofgreater than 2 MPa. Such cohesive values allow said polymer to be usedas adhesive, for example as leaktightness seal on an ordinary support(concrete, glass, marble), in the building industry, or alternativelyfor the bonding of glazings in the motor vehicle and naval industries.

According to a preferred variant, the main chain of the copolymer Pconsists essentially of the repeating unit (I) of formula (I), of therepeating unit (II) of formula (II) and, optionally, of the repeatingunit (III) of formula (III). Thus, the number of units (I), (II) and,optionally, (III) advantageously represents at least 90% of the totalnumber of constituent units of the main chain of the copolymer P, andeven more advantageously at least 95%.

According to a preferred variant, the main chain of the copolymer Pconsists essentially of the repeating unit (I) of formula (I) and of therepeating unit (II) of formula (II).

According to a more preferred variant, the relative proportion of unitsof formula (I) and of units of formula (II) present in the main chain ofthe copolymer P corresponds to an excess of units of formula (I). Moreparticularly, the number p of units (I) and the number n of units (II)are such that:

-   -   p/(n+p) is between 45% and 95%, and    -   n/(n+p) is between 5% and 55%.

The latter parameters may be determined analytically by ¹H and ¹³C NMRspectroscopy.

According to a first embodiment, which is more preferred, of thecopolymer P according to the invention, all the bonds

that are represented in formulae (I), (II) and, optionally, (III) andalso in the formulae giving the meaning of R⁰ are carbon-carbon doublebonds.

According to this first embodiment, the main chain of the copolymer P isthus such that:

-   -   the unit (I) also has the formula (I′):

-   -   the unit (II) also has the formula (II′):

in which R⁰ represents a methyl radical or one of the three radicalshaving the following formula:

-   -   and, optionally, the unit (III) also has the formula (III′):

it being pointed out that, in the above formulae, the

bond is a single bond geometrically oriented on one side or the otherrelative to the double bond (cis or trans).

The corresponding units of the main chain of the copolymer P are thenthemselves connected via a carbon-carbon double bond.

According to a most particularly preferred variant of this firstembodiment of the invention, the main chain of the copolymer P is suchthat:

-   -   on the p units of formula (I′), p″ also correspond to formula        (I″), p″ being an integer other than 0, less than p and such        that p″/p is greater than 0.8:

and

-   -   on the n units of formula (II′), n″ also correspond to formula        (II″), n″ being an integer other than 0, less than n and such        that n″/n is greater than 0.9:

In accordance with this embodiment, at least 80% of the units of formula(I′) are of cis configuration, represented by formula (I″), and at least90% of the units of formula (II′) are also of cis configuration,represented by formula (II″). The corresponding percentages may bedetermined by ¹H and ¹³C NMR.

According to another variant of this first embodiment, m is equal to 0and the main chain of P does not comprise any units of formula (III′).

According to a second embodiment of the copolymer P according to theinvention, all the bonds

that are represented in formulae (I), (II) and, optionally, (III) andalso in the formulae giving the meaning of R⁰ are carbon-carbon singlebonds.

According to this second embodiment, the main chain of the copolymer Pis thus such that:

-   -   the unit (I) also has the formula (I^(H)):

-   -   the unit (II) also has the formula (II^(H)):

in which R⁰ represents a methyl radical or one of the three radicalshaving the following formula:

-   -   and, optionally, the unit (III) has the formula (III^(H)):

The copolymer P according to this second embodiment is derived, forexample, from the hydrogenation of the copolymer P according to thefirst embodiment described above.

According to an even more preferred variant of each of these twoembodiments, the radical R⁰ of the unit (II) represents a methylradical.

As now regards the end groups of cyclocarbonate and similar type of thecopolymer P according to the invention, and according to a firstembodiment:

-   -   F¹ is: G1-O—(O═C)—(CH₂)_(g)— and also has the formula:

and

-   -   F² is: —(CH₂)_(d)—C(═O)—O-D1 and also has the formula:

corresponding to a cyclocarbonate (or 2-oxo-1,3-dioxolan-4-yl) endgroup.

According to a preferred variant of said mode, A¹ is a methylene group.

According to another preferred variant of said mode, g and d areidentical and equal to 0 or 1.

According to a second embodiment:

-   -   F¹ is: G2-O—(O═C)—(CH₂)_(g)— and also has the formula:

-   -   F² is: —(CH₂)_(d)—C(═O)—O-D2 and also has the formula:

corresponding to a dithiocyclocarbonate (or2-thione-1,3-oxathiolan-4-yl) end group.

According to a preferred variant of said mode, A² is a methylene group.

According to another preferred variant of said mode, g and d areidentical and equal to 0 or 1.

According to a third embodiment:

-   -   F¹ is: G3-O—(O═C)—(CH₂)_(g)— and also has the formula:

-   -   F² is: —(CH₂)_(d)—C(═O)—O-D3 and also has the formula:

corresponding to an exo-vinylene cyclocarbonate end group.

According to a preferred variant of said mode, A³ is a —(CH₂)₂— group,A⁴ is a hydrogen atom and A⁵ and A⁶ are each a methyl.

According to another preferred variant of said mode, g and d areidentical and equal to 0 or 1.

According to a fourth embodiment:

-   -   F¹ is: G4-O—(O═C)—(CH₂)_(g)— and also has the formula:

-   -   F² is: —(CH₂)_(d)—C(═O)—O-D4 and also has the formula:

corresponding to an exo-vinylene cyclocarbonate end group.

According to a preferred variant of said mode, A⁷ is a propylene groupand A⁸ is a methyl.

According to another preferred variant of said mode, g and d areidentical and equal to 0 or 1.

According to a fifth embodiment:

-   -   F¹ is: G5-O—(O═C)—(CH₂)_(g)— and also has the formula:

-   -   F² is: —(CH₂)_(d)—C(═O)—O-D5 and also has the formula:

corresponding to a 2-oxo-1,3-dioxolen-4-yl end group.

According to a preferred variant of said mode, A⁹ is a hydrogen atom andA¹⁰ is a methyl.

According to another preferred variant of said mode, g and d areidentical and equal to 0 or 1.

The invention also relates to a process for preparing thehydrocarbon-based copolymer P as defined previously, said processcomprising:

(i) a step of heating at a temperature ranging from 30° C. to 80° C.:

-   -   (a) of a statistical bipolymer A chosen from a        poly(butadiene-isoprene), a poly(butadiene-myrcene) and a        poly(butadiene-farnesene); and    -   (b) optionally in the presence of a compound B of formula (B):

and then

(ii) a step of heating the product formed in step (i) to a temperaturein a range from 20 to 60° C., in the presence of a chain-transfer agent(also referred to as CTA), it being pointed out that:

-   -   (c) when said hydrocarbon-based copolymer P is such that the        pair (G, D) is (G1, D1), (G3, D3), (G4, D4) or (G5, D5), then        said CTA is a compound of formula (C1) or (C2):

in which:

-   F¹ and F² are such that the pair (G, D) corresponds to the    corresponding definition (G1, D1), (G3, D3), (G4, D4) or (G5, D5);-   the    bond is a carbon-carbon single bond geometrically oriented on one    side or the other relative to the double bond (cis or trans); and    -   (d) when said hydrocarbon-based copolymer P is such that the        pair (G, D) is (G2, D2), then said CTA is the diepoxy compound        of formula (C′1) or (C′2):

in which:

-   F′¹e and F′²e are monovalent radicals of formulae (G′) and (D′):

-   the    bond is a carbon-carbon single bond geometrically oriented on one    side or the other relative to the double bond (cis or trans);    it also being pointed out that each of the steps (i) and (ii) is    performed in the presence of a metathesis catalyst and of a solvent;    -   and then

(iii) when said hydrocarbon-based copolymer P is such that the pair (G,D) is (G2, D2), a step of dithiocarbonation of the polymer obtained instep (ii), by reaction with carbon disulfide (CS₂) in the presence of ahalogenated lithium compound, at a temperature ranging from 10 to 45° C.

Each of the steps (i), (ii) and (iii) is described below in greaterdetail.

Step (i):

Step (i) involves a depolymerization reaction of the bipolymer A andintramolecular cyclization, which leads to the formation of one (ormore) macrocyclic cooligomer O comprising:

-   -   the unit of formula (I′) repeated p′⁰ times, p′⁰ being an        integer other than 0;    -   the unit of formula (II′) repeated n′⁰ times, n′⁰ being an        integer other than 0;    -   and, optionally, the unit of formula (III′) repeated m′⁰ times,        m′⁰ being an integer greater than or equal to 0;

it being pointed out that p′⁰, n′⁰ and m′⁰ are such that thenumber-average molecular mass Mn of the cyclic cooligomer(s) O is in arange extending from 162 to 5000 g/mol, preferably from 1000 to 3000g/mol.

The formation and the structure of the macrocyclic cooligomer(s) O maybe characterized by size exclusion chromatography (or SEC) and massspectrometry techniques. The distribution in the macrocycle of the unitsof formulae (I′), (II′) and optionally (III′) is statistical.

A preferred temperature range for the heating of the bipolymer A and,optionally, of compound B, according to step (i) ranges from 30° C. to60° C.

The corresponding heating time is adapted to obtain a yield close to100% relative to the molar amount of bipolymer A used, and also that ofthe other reagents present. A time ranging from 1 hour to 8 hours,preferably from 1 to 3 hours, is generally suitable.

Bipolymer A:

The bipolymer A is a copolymer which essentially consists of twomonomers and is chosen from a poly(butadiene-isoprene), apoly(butadiene-myrcene) and a poly(butadiene-farnesene).

According to a first variant, which is most particularly preferred, ofthe process according to the invention, the bipolymer A used in step (i)is a poly-(butadiene-isoprene). A hydrocarbon-based copolymer Paccording to the invention is then advantageously obtained:

-   -   either on conclusion of step (ii) when P is such that the pair        (G, D) is (G1, D1), (G3, D3), (G4, D4) or (G5, D5),    -   or on conclusion of step (iii) when P is such that the pair        (G, D) is (G2, D2). The main chain of P comprises, according to        this same variant:    -   the repeating unit of formula (I′) and    -   the repeating unit of formula (II′) in which R⁰ represents a        methyl radical.

The poly(butadiene-isoprene) polymers are copolymers which constitute anindustrially advantageous starting material, notably on account of theiravailability and of their properties in terms of industrial hygiene. Thepoly(butadiene-isoprene) polymers are generally obtained via variousprocesses of polymerization:

-   -   of 1,3-butadiene of formula: H₂C═CH—CH═CH₂, and    -   2-methylbuta-1,3-diene (or isoprene), of formula:        H₂C═C(CH₃)—CH═CH₂.

The polymerization of 1,3-butadiene may be performed according to atrans-1,4 addition or a cis-1,4 addition, resulting in a repeating unitin the copolymer chain (designated, respectively, by trans-1,4 andcis-1,4 butadiene unit), which is in the form of the two geometricalisomers having the respective formulae:

The cis-1,4 butadiene unit is identical to the unit of formula (I″)defined previously.

The polymerization of 1,3-butadiene may also be performed according to a1,2-addition, resulting in a repeating unit in the copolymer chain(designated by vinyl-1,2 butadiene unit) which has the formula:

Thus, the poly(butadiene-isoprene) generally comprises in its chain theabove three repeating units, designated hereinbelow generically by“butadiene-based units”.

Similarly, the polymerization of isoprene may be performed according toa trans-1,4 addition or a cis-1,4 addition, resulting in a repeatingunit in the copolymer chain (designated, respectively, by trans-1,4 andcis-1,4 isoprene unit), which is in the form of the two geometricalisomers having the respective formulae:

The cis-1,4 isoprene unit is identical to the unit of formula (II″) inwhich R⁰ is a methyl, as defined previously.

The polymerization of isoprene may also be performed according to a1,2-addition, resulting in a repeating unit in the copolymer chain(designated by vinyl-1,2 isoprene unit) which has the formula:

The polymerization of isoprene may, finally, be performed according to a3,4-addition, resulting in a repeating unit in the copolymer chain(designated by vinyl-3,4 isoprene unit) which has the formula:

Thus, the poly(butadiene-isoprene) generally comprises in its chain theabove four repeating units, designated hereinbelow generically by“isoprene-based units”.

The poly(butadiene-isoprene) used in step (i) may have a number-averagemolecular mass (Mn) ranging from 3000 to 100 000 g/mol, preferably from3000 to 50 000 g/mol, and a glass transition temperature (Tg) rangingfrom −110 to −60° C.

It preferably comprises from 45% to 95% by number of butadiene-basedunits and from 5% to 55% by number of isoprene-based units, saidpercentages being expressed on the basis of the total number ofconstituent units of the poly(butadiene-isoprene) chain.

Preferably, the chain of the poly(butadiene-isoprene) used in step (i)comprises:

-   -   less than 5% by number of vinyl-1,2 butadiene units on the basis        of the number of butadiene-based units, and    -   less than 5% of the total number of vinyl-1,2 isoprene units and        of vinyl-3,4 isoprene units on the basis of the number of        isoprene-based units.

Even more preferentially, this twofold limit greater than 5 mol % islowered to 2%.

According to another variant, which is most particularly preferred, thechain of the poly(butadiene-isoprene) used in step (i) comprises:

-   -   at least 80% by number of cis-1,4 butadiene units on the basis        of the number of butadiene-based units, and    -   at least 90% by number of cis-1,4 isoprene units on the basis of        the number of isoprene-based units.

In accordance with this last variant, such a poly(butadiene-isoprene),which is liquid at room temperature, is often termed as having “a highcontent of cis-1,4 butadiene and cis-1,4 isoprene units” and is alsoreferred to by the term “high cis poly(butadiene-isoprene)”. Thepreferred variant of the copolymer P corresponding to the presence ofthe units of formulae (I″) and (II″), as defined previously, is thenadvantageously obtained, either on conclusion of step (ii) or onconclusion of step (iii) depending on the meaning of the pair (G, D) asspecified above.

The percentages by number of vinyl-1,2 butadiene, vinyl-1,2 isoprene,vinyl-3,4 isoprene, cis-1,4 butadiene and cis-1,4 isoprene units,defined above, may be determined by ¹H and ¹³C NMR.

An example of such a poly(butadiene-isoprene) that may be mentioned isKuraprene® LIR-390, which is commercially available from the companyKuraray.

This liquid poly(butadiene-isoprene) has a number-average molecular mass(Mn) equal to 48 000 g/mol. It comprises 92% by number ofbutadiene-based units and 8% by number of isoprene-based units, saidpercentages being expressed on the basis of the total number ofconstituent butadiene-based and isoprene-based units in the chain.

It also comprises:

-   -   on the basis of the number of butadiene-based units, about 1% by        number of vinyl-1,2 butadiene units, and    -   on the basis of the number of isoprene-based units, about 1% by        number of vinyl-1,2 isoprene units and less than 1% by number of        vinyl-3,4 isoprene units.

It finally comprises:

-   -   about 85% by number of cis-1,4 butadiene units on the basis of        the number of butadiene-based units, and    -   about 98% by number of cis-1,4 isoprene units on the basis of        the number of isoprene-based units.

Another example of a poly(butadiene-isoprene) that may be mentioned isKuraprene® LIR-340, which is also commercially available from thecompany Kuraray.

This poly(butadiene-isoprene) has a number-average molecular mass (Mn)equal to 34 000 g/mol. It comprises 46% by number of butadiene-basedunits and 54% by number of isoprene-based units, said percentages beingexpressed on the basis of the total number of constituent units in thechain. It moreover has the same characteristics as those indicatedpreviously for Kuraprene® LIR-390.

According to a second variant of the process according to the invention,the bipolymer A is either a poly(butadiene-myrcene) or apoly(butadiene-farnesene).

Myrcene is a natural organic compound belonging to the chemical familyof monoterpenes and is an important intermediate in the fragranceindustry. It is produced semi-synthetically from plants of the genusMyrcia. It is in the form of two geometrical isomers:

-   -   α-myrcene, having the structural formula:

-   -   β-myrcene, having the structural formula:

Farnesene or β-farnesene is a natural isoprenoid compound which may bechemically synthesized by oligomerization of isoprene or by dehydrationof neridol. It is mainly used as a fragrance or intermediate andcorresponds to the structural formula:

Reference is made to patent application EP 2810963 for the processes forpreparing copoly(butadiene-myrcene) and copoly(butadiene-farnesene).

A hydrocarbon-based copolymer P according to the invention is obtainedin this second variant (either on conclusion of step (ii) or onconclusion of step (iii) depending on the meaning of the pair (G, D) asstated above), the main chain of which copolymer comprises:

-   -   the repeating unit of formula (I′) and    -   the repeating unit of formula (II′) in which R⁰ represents:        -   the radical of formula:

corresponding to α-myrcene;

corresponding to β-myrcene; or

corresponding to β-farnesene.

Compound of Formula (B):

The use in step (i) of the compound of formula (B) advantageously leadsto the production of copolymers P according to the invention whose mainchain comprises the additional unit of formula (III′), as definedpreviously.

The compound of formula (B) generally comprises from 6 to 30 andpreferably from 6 to 22 carbon atoms.

Preferably:

-   -   R¹, R², R³ and R⁴ represent a hydrogen atom or an alkyl or        alkoxycarbonyl radical comprising from 1 to 14 and even more        preferentially from 1 to 8 carbon atoms;    -   the radical R⁶ included in the group —NR⁶, which is one of the        meanings of R⁵, is a linear radical comprising from 1 to 14        carbon atoms.

According to an even more preferred variant:

-   -   at most one of the groups taken from (R¹, R², R² and R⁴) is a        C₁-C₈ alkoxycarbonyl radical and all the others represent a        hydrogen atom; and/or    -   R⁵ represents a —CH₂— radical or an oxygen atom.

The compound of formula (B) is notably chosen from:

-   -   norbornene, of the following formula:

-   -   norbornadiene, of the following formula:

-   -   dicyclopentadiene, of the following formula:

-   -   7-oxanorbornene, of the following formula:

-   -   7-oxanorbornadiene, of the following formula:

-   -   5-ethylidene-2-norbornene, of the following formula:

-   -   or 5-norbornene-2-methyl acetate, of the following formula:

The compound of formula (B) may also be chosen from the compounds havingthe following formulae:

in which R is an alkyl radical comprising from 1 to 22 carbon atoms,preferably from 1 to 14 carbon atoms.

The compound of formula (B) may also be chosen from the group formed bythe addition products (or adducts) resulting from the Diels-Alderreaction using cyclopentadiene or furan as starting material, and alsonorbornene-based compounds, such as the branched norbornenes asdescribed in WO 2001/04173 (such as: norbornene isobornyl carboxylate,norbornene phenyl carboxylate, norbornene ethylhexyl carboxylate,norbornene phenoxyethyl carboxylate and alkyl norbornene dicarboximide,the alkyl usually including from 3 to 8 carbon atoms), and thesubstituted norbornenes as described in WO 2011/038057 (norbornenedicarboxylic anhydrides and optionally 7-oxanorbornene dicarboxylicanhydrides).

Among the various compounds mentioned of formula (B), the ones mostparticularly preferred are norbornene and dicyclopentadiene.

Step (ii):

The macrocyclic cooligomers O corresponding to the product formed instep (i) are polymerized by heating to a temperature in a range from 20to 60° C., in the presence of a chain-transfer agent (also referred toas CTA).

For the preparation of a hydrocarbon-based copolymer P such that thepair (G, D) is (G1, D1), (G3, D3), (G4, D4) or (G5, D5), then said CTAis a compound of formula (C1) or (C2):

in which:

-   F¹ and F² are such that the pair (G, D) corresponds to the    corresponding definition (G1, D1), (G3, D3), (G4, D4) or (G5, D5);-   the    bond is a carbon-carbon single bond geometrically oriented on one    side or the other relative to the double bond (cis or trans).

A hydrocarbon-based copolymer P according to the invention is obtainedin this case directly on conclusion of step (ii).

When a CTA of formula (C1) is used, the corresponding process is oftentermed a “monofunctional CTA route”. When a CTA of formula (C2) is used,the corresponding process is often termed a “difunctional CTA route”.

For the preparation of a hydrocarbon-based copolymer P such that thepair (G, D) is (G2, D2), then said CTA is the diepoxy compound offormula (C′1) or (C′2):

in which:

-   -   F′¹e and F′²e are monovalent radicals of formulae (G′) and (D′):

-   -   the        bond is a carbon-carbon single bond geometrically oriented on        one side or the other relative to the double bond (cis or        trans).

An intermediate hydrocarbon-based copolymer I comprising the two endgroups F′¹e and F′²e, and the main chain of which is identical to thatof the copolymer P according to the invention, is obtained in this casedirectly on conclusion of step (ii).

CTA of Formula (C1) or (C2):

CTA of Formula (C1) or (C2) in which the Pair (G, D) is (G1, D1):

According to a first embodiment (monofunctional CTA route), the CTA hasthe formula (C1) in which F² is such that D is D1.

Said CTA then has the formula:

This compound may be manufactured according to the procedure describedin patent application EP 0 683 163 in the name of Mitsubishi GasChemical or according to the procedure described in Polymer Chemistry,2013, 4, 1313-1316 by L. Annunziata, S. Fouquay, G. Michaud, F. Simon,S. Guillaume and J-F. Carpentier.

According to a preferred variant of this embodiment, d is equal to 0.

According to another preferred variant of this embodiment, A¹ is amethylene group.

The CTA corresponding to the combination of these two preferred variantshas the formula:

and is referred to hereinbelow as CTA¹.

According to a second embodiment (difunctional CTA route), the CTA hasthe formula (C2) in which F¹ and F² are such that the pair (G, D) is(G1, D1).

Said CTA then has the formula:

This compound may be manufactured according to the procedure describedin Polymer Chemistry, 2013, 4, 1313-1316 by L. Annunziata, S. Fouquay,G. Michaud, F. Simon, S. Guillaume and J-F. Carpentier, in which acrylicacid has been replaced with the carboxylic acids corresponding to thepresent invention.

According to a preferred variant of this embodiment, g=1 or d=1 and evenmore preferably: g=d=1.

According to another preferred variant of this embodiment, A¹ is amethylene group.

The CTA corresponding to the combination of these two preferred variantshas the formula:

and is referred to hereinbelow as CTA².

CTA of Formula (C1) or (C2) in which the Pair (G, D) is (G3, D3):

According to a first embodiment (monofunctional CTA route), the CTA hasthe formula (C1) in which F² is such that D is D3.

Said CTA then has the formula:

This compound may be manufactured according to the procedure describedin patent application WO 2013/144299 in the name of BASF and WO2016/185106 in the name of Bostik.

According to a preferred variant of this embodiment, d is equal to 0.

According to other preferred variants of this embodiment:

-   -   A³ is a —(CH₂)₂— group, and/or    -   A⁴ is a hydrogen atom, and/or    -   A⁵ and A⁶ are each a methyl radical.

The CTA corresponding to the combination of these four preferredvariants has the formula:

and is referred to hereinbelow as CTA³.

According to a second embodiment (difunctional CTA route), the CTA hasthe formula (C2) in which F¹ and F² are such that the pair (G, D) is(G3, D3).

Said CTA then has the formula:

This compound may be manufactured according to the procedure describedin patent application WO 2016/162627 in the name of Bostik.

According to a preferred variant of this embodiment, g=1 or d=1 and evenmore preferably: g=d=1.

According to other preferred variants of this embodiment:

-   -   A³ is a —(CH₂)₂— group, and/or    -   A⁴ is a hydrogen atom, and/or    -   A⁵ and A⁶ are each a methyl radical.

The CTA corresponding to the combination of these four preferredvariants has the formula:

and is referred to hereinbelow as CTA⁴.

CTA of Formula (C1) or (C2) in which the Pair (G, D) is (G4, D4):

According to a first embodiment (monofunctional CTA route), the CTA hasthe formula (C1) in which F² is such that D is D4.

Said CTA then has the formula:

This compound may be manufactured according to the procedure describedin patent application WO 2016/169858 in the name of BASF.

According to a preferred variant of this embodiment, d is equal to 0.

According to other preferred variants of this embodiment:

-   -   A⁷ is a propylene radical, and/or    -   A⁸ is a methyl radical.

The CTA corresponding to the combination of these three preferredvariants has the formula:

and is referred to hereinbelow as CTA⁵.

According to a second embodiment (difunctional CTA route), the CTA hasthe formula (C2) in which F¹ and F² are such that the pair (G, D) is(G4, D4).

Said CTA then has the formula:

This compound may be manufactured according to the procedure describedin patent application WO 2016/169858 from BASF, in which acrylic acidhas been replaced with the dicarboxylic acids corresponding to thepresent invention.

According to a preferred variant of this embodiment, g=1 or d=1 and evenmore preferably: g=d=1.

According to other preferred variants of this embodiment:

-   -   A⁷ is a propylene radical, and/or    -   A⁸ is a methyl radical.

The CTA corresponding to the combination of these three preferredvariants has the formula:

and is referred to hereinbelow as CTA⁶.

CTA of Formula (C1) or (C2) in which the Pair (G, D) is (G5, D5):

According to a first embodiment (monofunctional CTA route), the CTA hasthe formula (C1) in which F² is such that D is D5.

Said CTA then has the formula:

According to a preferred variant of this embodiment, d is equal to 0.

According to other preferred variants of this embodiment:

-   -   A⁹ is a hydrogen atom, and/or    -   A¹⁰ is a methyl radical.

The CTA corresponding to the combination of these three preferredvariants has the formula:

and is referred to hereinbelow as CTA⁷.

According to a second embodiment (difunctional CTA route), the CTA hasthe formula (C2) in which F¹ and F² are such that the pair (G, D) is(G5, D5).

Said CTA then has the formula:

According to a preferred variant of this embodiment, g=1 or d=1 and evenmore preferably: g=d=1.

According to other preferred variants of this embodiment:

-   -   A⁹ is a hydrogen atom, and/or    -   A¹⁰ is a methyl radical.

The CTA corresponding to the combination of these two preferred variantshas the formula:

and is referred to hereinbelow as CTA⁸.

The compounds corresponding to the general formulae of these last twoembodiments may be obtained according to the procedure described inpatent application U.S. Pat. No. 7,041,820 from Nippon Sodsa and DaiichiAsubio Pharma by reacting, in solvent medium and in the presence of aphase-transfer catalyst (for example a metal iodide), an alkaline saltof a monocarboxylic or dicarboxylic acid with a precursor of4-halomethyl-5-alkyl-1,3-dioxolen-2-one type:

In the above scheme:

-   -   Q is a monovalent radical (f equal to 1) or divalent radical (f        equal to 2) having the respective structures:

and

-   -   X is a chlorine or bromine atom.

The precursor of 4-halomethyl-5-alkyl-1,3-dioxolen-2-one type may beobtained by following procedures described in patent application EP 0078 413 from Kanebo.

CTA of Formula (C′1) or (C′2) Used for the Preparation of the CopolymerP Such that the Pair (G, D) is (G2, D2):

According to a first embodiment (monofunctional CTA route), the CTA hasthe formula (C′1), which, given the meaning of F′^(2e), may also berepresented by the following general formula:

This compound may be manufactured according to the procedure describedin patent application CN 102 757 409 in the name of Hunan RocketChemical Materials or patent application EP 0 683 163 in the name ofMitsubishi Gas Chemical.

According to a preferred variant of this embodiment, d is equal to 0.

According to another preferred variant of this embodiment, A² is amethylene group.

The CTA corresponding to the combination of these two preferred variantshas the formula:

and is referred to hereinbelow as CTA⁹.

According to a second embodiment (difunctional CTA route), the CTA hasthe formula (C′2), which, given the meaning of F′¹e and F′²e, may alsobe represented by the following general formula:

This compound may be manufactured according to the procedure describedin patent application EP 0 336 670 in the name of Hoechst, in whichmuconic acid has been replaced with the dicarboxylic acids correspondingto the present invention.

According to a preferred variant of this embodiment, g=1 or d=1 and evenmore preferably: g=d=1.

According to another preferred variant of this embodiment, A² is amethylene group.

The CTA corresponding to the combination of these two preferred variantshas the formula:

and is referred to hereinbelow as CTA¹⁰.

Without being bound by any reaction mechanism, it is estimated that step(ii) involves a polymerization by opening of the macrocycles O and across-metathesis with the CTA.

This step (ii) advantageously has low exothermicity, and as such theindustrial implementation of the process according to the invention doesnot pose any temperature control difficulties.

The molar amount of CTA to be introduced into the present step (ii) islinked to the molar amount of bipolymer A and, optionally, to the molaramount of compound B introduced into step (i).

These molar amounts are such that the ratio r which is equal to theratio of the number of moles of said CTA:

-   -   to the number N_((A)) of moles of the bipolymer A, in the case        where said bipolymer A is the only reagent used in step (i), or    -   to the sum of N_((A)) and of the number of moles N_((B)) of the        compound of formula (B), in the case where the compound of        formula (B) is also used in step (i),

is in an interval ranging from 0.0010 to 1.0.

Thus, when, in accordance with a preferred variant of the processaccording to the invention, the bipolymer A is apoly(butadiene-isoprene), said ratio r is equal to the ratio of thenumber of moles of the CTA:

-   -   to the number N_((A)) of moles of said poly(butadiene-isoprene),        in the case where said poly(butadiene-isoprene) is the only        reagent used in step (i), or    -   to the sum of N_((A)) and of the number of moles N_((B)) of the        compound of formula (B), in the case where the compound of        formula (B) is also used in step (i).

Even more preferably, the ratio r defined above is in an intervalranging from 0.0020 to 0.3.

Metathesis Catalyst and Solvent Used in Steps (i) and (ii):

Steps (i) and (ii) of the process according to the invention eachinvolve a metathesis catalyst and a solvent which may be identical ordifferent, and preferably identical in each of these two steps.

The metathesis catalyst is preferably a ruthenium-based catalyst andeven more preferably a Grubbs catalyst.

Such a catalyst is generally a commercial product.

The metathesis catalyst is generally a transition metal catalyst,notably including a ruthenium-based catalyst, generally in the form ofruthenium complex(es), such as a ruthenium-carbene complex.

According to the invention, the term “Grubbs catalyst” generally means a1^(st) or 2^(nd) generation Grubbs catalyst, but also any other catalystof Grubbs type (of ruthenium-carbene type) or Hoveyda-Grubbs typeaccessible to a person skilled in the art, for instance the substitutedGrubbs catalysts described in U.S. Pat. No. 5,849,851.

A 1^(st) generation Grubbs catalyst is generally of formula (G1):

in which Ph is phenyl, Cy is cyclohexyl and the group P(Cy)₃ is atricyclohexylphosphine group.The IUPAC name of this compound is:benzylidenebis(tricyclohexylphosphine)dichlororuthenium (of CAS number:172222-30-9). Such a catalyst is notably available from the companyAldrich.

A 2^(nd) generation (or G2) Grubbs catalyst that is preferred isgenerally of formula (G2):

in which Ph is phenyl and Cy is cyclohexyl.The IUPAC name of the second generation of this catalyst isbenzylidene[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(tricyclohexylphosphine)ruthenium(of CAS number: 246047-72-3). This catalyst is also available from thecompany Aldrich.

The solvent is generally chosen from the group formed by the aqueous ororganic solvents typically used in polymerization reactions and whichare inert under the polymerization conditions, such as aromatichydrocarbons, chlorinated hydrocarbons, ethers, aliphatic hydrocarbons,alcohols, water or mixtures thereof.

A preferred solvent is chosen from the group formed by benzene, toluene,para-xylene, methylene chloride (or dichloromethane),1,2-dichloroethane, dichlorobenzene, chlorobenzene, tetrahydrofuran,diethyl ether, pentane, hexane, heptane, a mixture of liquidisoparaffins (for example Isopar®), methanol, ethanol, water or mixturesthereof.

Even more preferably, the solvent is chosen from the group formed bybenzene, toluene, para-xylene, methylene chloride, 1,2-dichloroethane,dichlorobenzene, chlorobenzene, tetrahydrofuran, diethyl ether, pentane,hexane, heptane, methanol, ethanol or mixtures thereof.

Even more particularly preferably, the solvent is dichloromethane,1,2-dichloroethane, toluene, heptane or a mixture of toluene and1,2-dichloroethane.

It is also possible for each of the steps (i) and (ii) to be performedwithout solvent.

The main chain of the hydrocarbon-based copolymer P according to theinvention that is obtained directly on conclusion of steps (i) and (ii)is unsaturated, and, more precisely, comprises—in accordance with thefirst embodiment described previously for said copolymer—a unit (I) offormula (I′) repeated p′ times, a unit (II) of formula (II′) repeated n′times and, optionally, a unit (III) of formula (III′) repeated m′ times.

Step (iii):

In accordance with the process for preparing a hydrocarbon-basedcopolymer P such that the pair (G, D) is (G2, D2), either the monoepoxyCTA of formula (C′1) or the diepoxy CTA of formula (C′2) is used in step(ii). An intermediate hydrocarbon-based copolymer I comprising the twoend groups F′¹e and F′²e, having the respective formulae (G′) and (D′),and the main chain of which is identical to that of the copolymer Paccording to the invention, is obtained in this case directly onconclusion of step (ii).

Said intermediate copolymer I is then reacted, in accordance with thepresent step (iii) in a dithiocarbonation with carbon disulfide (CS₂) inthe presence of a halogenated lithium compound, at a temperature rangingfrom 10 to 45° C.

At the end of this reaction, the hydrocarbon-based copolymer P such thatthe pair (G, D) is (G2, D2) is then obtained.

The process for preparing the hydrocarbon-based copolymer P that hasjust been described may also comprise, besides steps (i) and (ii), andoptionally (iii), an additional step of hydrogenation of the doublebonds.

This step is generally performed by catalytic hydrogenation, usuallyunder hydrogen pressure and in the presence of a hydrogenation catalyst,such as a catalyst of palladium supported on carbon (Pd/C). It makes itpossible more particularly to obtain for the hydrocarbon-based copolymerP—in accordance with the second embodiment described previously for saidcopolymer—a main chain which is saturated, and which thus comprises aunit (I) of formula (I^(H)) repeated p times, a unit (II) of formula(II^(H)) repeated n times and, optionally, a unit (III) of formula(III^(H)) repeated m times.

Finally, according to a preferred variant of the process for preparingthe hydrocarbon-based copolymer P, the CTA used in step (ii) is adifunctional CTA of formula (C2) or (C′2). Said copolymer P is thenobtained in an improved yield.

The invention also relates to the use, as adhesive, of thehydrocarbon-based polymer comprising two end groups of cyclocarbonate orsimilar type, as defined previously, as a mixture with an amine compoundcomprising at least two amine groups, for example chosen from diamines,triamines and higher homologues. The amounts of the hydrocarbon-basedpolymer and of the amine compound correspond to stoichiometric amounts,i.e. the mole ratio of the number of cyclocarbonate (or similar) groupsto the number of amine groups ranges from 0.8 to 1.2, preferably from0.9 to 1.1, or even is about 1.0.

In practice, the hydrocarbon-based polymer and the amine compound, usedas curing agent, are advantageously each included in a component of atwo-component composition which is made available to the user. Said userthus, at the time of use of the adhesive, mixes these two components,optionally under hot conditions, so as to obtain a liquid adhesivecomposition of suitable viscosity.

The invention also relates to a process for assembling two substrates bybonding, comprising:

-   -   coating at least one of the two substrates to be assembled with        a liquid adhesive composition obtained by mixing an amine        compound comprising at least two amine groups with the        hydrocarbon-based polymer comprising two end groups of        cyclocarbonate or similar type as defined previously; and then    -   actually bringing the two substrates into contact.

The liquid adhesive composition is either the adhesive compositioncomprising said compound and said polymer in the liquid state at roomtemperature, or the hot-melt adhesive composition. A person skilled inthe art is capable of working so that the adhesive composition used isin liquid form and at a suitable viscosity at the time of its use.

Coating with the liquid adhesive composition is preferably performed inthe form of a layer with a thickness within a range from 0.3 to 5 mm,preferably from 1 to 3 mm, on at least one of the two surfaces whichrespectively belong to the two substrates to be assembled and which areintended to be brought into contact with each other along a contactsurface. The actual bringing into contact of the two substrates is thenperformed along their contact surface.

Needless to say, the coating operation and the contacting operation haveto be performed within a compatible time interval, as is well known tothose skilled in the art, i.e. before the adhesive layer applied to thesubstrate loses its ability to attach, by adhesive bonding, thissubstrate to another substrate. In general, the polycondensation of thehydrocarbon-based polymer with the amine compound begins to take placeduring the coating operation and then continues to take place during thestep in which the two substrates are brought into contact.

The appropriate substrates are, for example, inorganic substrates, suchas glass, ceramics, concrete, metals or alloys (such as aluminiumalloys, steel, non-ferrous metals and galvanized metals); or elseorganic substrates, such as wood, plastics, such as PVC, polycarbonate,PMMA, polyethylene, polypropylene, polyesters or epoxy resins;substrates made of metal and composites coated with paint (as in themotor vehicle field).

The examples that follow are given purely by way of illustration of theinvention and should not be interpreted in order to limit the scopethereof.

The copolymers P illustrated have a Brookfield viscosity at 23° C. ofless than 50 Pa·s.

EXAMPLE 1 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Hot Cross-Metathesis in thePresence of CTA¹ (Monofunctional CTA Route) and Production of aCopolymer P Such That (G, D) is (G1, D1)

Kuraprene® LIR-390 as defined previously is used as liquidpoly(butadiene-isoprene), and, as chain-transfer agent, the CTA¹ havingthe formula:

Step (i):

The poly(butadiene-isoprene) (81.00 mmol), benzoquinone (0.54 mmol) anddry CH₂Cl₂ (9 ml) are introduced into a 20 ml round-bottomed flask inwhich was also placed a Teflon®-coated magnetic stirring bar. The flaskand its contents are subsequently placed under argon.

The catalyst G2 defined previously (9.6 μmol) dissolved in CH₂Cl₂ (2 ml)is then added using a cannula.

This mixture is heated in an oil bath for 3 hours at 40° C. withstirring until the Kuraprene® LIR-390 has disappeared and a mixture ofmacrocyclic cooligomers O has formed, as attested to by size exclusionchromatography.

Step (ii):

The compound CTA¹ (0.27 mmol) is added by syringe and with stirring tothe mixture contained in the flask from step (i) and heating iscontinued at a temperature of 40° C.

The ratio r, as defined previously, is: 0.27/81.00, i.e. 0.003

After 8 hours, with effect from the addition of the CTA¹, the productpresent in the flask is extracted after evaporation of the solvent undervacuum. This product is then recovered in the form of a colourlessliquid, after precipitating from methanol, filtering and drying at 23°C. under vacuum, in a yield of greater than 90%.

Analysis by 1H/13C NMR gives the following results:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=2.25 (m,O—C(O)—O—CH—CH₂—O—C(O)—CH═CH—CH₂), 2.90 (d,O—C(O)—O—CH—CH₂—O—C(O)—CH═CH—CH₂), 4.30 and 4.63 (m,O—C(O)—O—CH₂—CH—CH₂—O—C(O)—CH═CH), 4.96 (m,O—C(O)—O—CH—CH₂—O—C(O)—CH═CH), 5.87 (m, O—C(O)—O—CH—CH₂—O—C(O)—CH═CH—),7.02 (m, O—C(O)—O—CH—CH₂—O—C(O)—CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=62.80 and 66.0O—C(O)—O—CH₂—CH—CH₂—O—C(O)—CH═CH, 74.1 O—C(O)—O—CH—CH₂—O—C(O)—CH═CH,122.2 O—C(O)—OCH—CH₂—O—C(O)—CH═CH, 50.9 O—C(O)—O—CH—CH₂—O—C(O)—CH═CH,154.7 O—C(O)—O—CH—CH₂—O—C(O)—CH═CH, 166.5 O—C(O)—O—CH—CH₂—O—C(O)—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17 020 g/mol and 2.7.

EXAMPLE 2 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA² (Difunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G1, D1)

Example 1 is repeated, without adding benzoquinone in step (i), andreplacing in step (ii), as chain-transfer agent, CTA¹ with CTA² offormula:

A polymer is also recovered, in a yield of greater than 90%, in the formof a colourless liquid, the ¹H/¹³C NMR analysis of which gives thefollowing values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=3.08 (d,O—C(O)—O—CH—CH₂—O—C(O)CH₂CH═CH), 4.36 (d,O—C(O)—O—CH—CH₂—O—C(O)—CH₂CH═CH), 4.53 (dd,O—C(O)—O—CH₂CHCH₂—O—C(O)—CH₂CH═CH), 4.66 (m,O—(O)—O—CH—CH₂—O—C(O)—CH₂CH═CH), 5.44 (m,O—C(O)—O—CH—CH₂—O—C(O)—CH₂—CH═CH—).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=37.4O—C(O)—O—CH—CH₂—O—C(O)—CH₂—CH═CH, 62.80 and 66.0O—C(O)—O—CH₂—CH—CH₂—O—C(O)—CH₂CH═CH, 74.1O—C(O)—O—CH—CH₂—O—C(O)CH₂CH═CH, 124.1 O—C(O)—O—CH—CH₂—O—C(O)—CH₂—CH═CH,130.8 O—C(O)—O—CH—CH₂—O—C(O)CH₂—CH═CH, 154.7O—C(O)—O—CH—CH₂—O—C(O)—CH₂CH═CH, 171.2 O—C(O)—O—CH—CH₂—O—C(O)—CH₂—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 16 990 g/mol and 2.7.

EXAMPLE 3 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA⁹ (Monofunctional CTA Route) and then Dithiocarbonation, andProduction of a Copolymer P Such That (G, D) is (G2, D2)

Steps (i) and (ii):

Example 1 is repeated, replacing, as chain-transfer agent, CTA¹ withCTA⁹ of formula:

Step (iii):

The isolated product, derived from steps (i) and (ii), lithium bromide(10.00 mmol) and dry THF (10 ml) were placed in a 20 ml round-bottomedflask in which was also placed a Teflon®-coated magnetic stirring bar.The flask and its contents were then placed under argon. Carbon sulfide(20.00 mmol) was then introduced dropwise by syringe into the flask. Theflask was then immersed in an oil bath at 40° C. for 17 hours. A productwas recovered after precipitating from methanol (20 ml), filtering anddrying at 23° C. under vacuum.

A polymer is also recovered in liquid form, the ¹H NMR/¹³C NMR analysisof which gives the following values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=2.25 (m,O—C(O)—O—CH—CH₂—O—C(O)—CH═CH—CH₂), 3.62 (d,O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH═CH), 2.86 (dd,O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH═CH), 5.39 (m,S—C(S)—O—CH—CH₂—O—C(O)—CH═CH), 5.87 (m, S—C(S)—O—CH—CH₂—O—C(O)—CH═CH),7.07 (m, S—C(S)—O—CH—CH₂—O—C(O)—CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=34.0O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH═CH, 66.7 O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH═CH,83.9 S—C(S)—O—CH—CH₂—O—C(O)—CH═CH, 122.2 S—C(S)—O—CH—CH₂—O—C(O)—CH═CH,150.9 S—C(S)—O—CH—CH₂—O—C(O)—CH═CH, 166.5 S—C(S)—O—CH—CH₂—O—C(O)—CH═CH,205.1 S—C(S)—O—CH—CH₂—O—C(O)—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo dithiocyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17,090 g/mol and 2.80.

EXAMPLE 4 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA¹⁹ (Difunctional CTA Route) and then Dithiocarbonation, andProduction of a Copolymer P Such That (G, D) is (G2, D2)

Example 3 is repeated, without adding benzoquinone in step (i), andreplacing in step (ii), as chain-transfer agent, CTA⁹ with CTA¹⁰ offormula:

A polymer in the form of a colourless liquid is also recovered onconclusion of step (iii) (i.e. after reaction of CS₂ with theunsaturated liquid polyolefin bearing epoxy end groups obtained fromstep (ii)), in a yield of greater than 90%, the ¹H/¹³C NMR analysis ofwhich polymer gives the following values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=3.04 (d,S—C(S)—O—CH—CH₂—O—C(O)—CH₂—CH═CH), 3.69 (dd,O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH₂—CH═CH), 4.37 (dd,O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH₂—CH═CH), 4.51 (m,S—C(S)—O—CH—CH₂—O—C(O)—CH₂CH═CH), 5.44 (m,S—C(S)—O—CH—CH₂—O—C(O)—CH₂CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=34.0O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH₂—CH═CH, 37.4S—C(S)—O—CH—CH₂—O—C(O)—CH₂—CH═CH, 34.0O—C(S)—S—CH₂CH—CH₂—O—C(O)—CH₂—CH═CH, 66.7O—C(S)—S—CH₂—CH—CH₂—O—C(O)—CH₂CH═CH, 83.9S—C(S)—O—CH—CH₂—O—C(O)—CH₂CH═CH, 124.1 S—C(S)—O—CH—CH₂—O—C(O)—CH₂—CH═CH,130.8 S—C(S)—O—CH—CH₂—O—C(O)—CH₂—CH═CH, 205.1S—C(S)—O—CH—CH₂—O—C(O)—CH₂CH═CH, 171.2 S—C(S)—O—CH—CH₂—O—C(O)—CH₂—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo dithiocyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17110 g/mol and 2.80.

EXAMPLE 5 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA³ (Monofunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G3, D3)

Example 1 is repeated, replacing, as chain-transfer agent, CTA¹ withCTA³ of formula:

A polymer is also recovered in liquid form, the ¹H NMR/¹³C NMR analysisof which gives the following values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=1.39 (s,O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH═CH), 2.25 (m,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH—CH₂), 4.43 (dd,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂CH═CH), 2.45 (m,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 5.90 (m,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH). 7.02 (m,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH═CH),

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=26.9O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 30.9O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 64.2O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 79.4O—C(O)—O—C(CH₃)₂—C═CH—CH₂CH₂—O—C(O)—CH═CH, 107.2O—C(O)—O—C═CH—CH₂CH₂—O—C(O)—CH═CH, 122.2O—C(O)—O—C═CH—CH₂—CH₂O—C(O)—CH═CH, 150.9O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 152.7O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 155.7O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 166.5O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formula:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17080 g/mol and 2.80.

EXAMPLE 6 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA⁴ (Difunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G3, D3)

Example 2 is repeated, replacing the CTA² with CTA⁴ of formula:

A polymer is also recovered in the form of a colourless liquid, in ayield of greater than 90%, the ¹H/¹³C NMR analysis of which gives thefollowing values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=1.39 (s,O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 2.59 (m,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂CH═CH), 3.08 (d,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 4.43 (dd,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 5.44 (m,O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH—), 6.13 (dd,O—C(O)—O—C═CH—O—CH₂—CH₂—O—C(O)—CH₂—CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=26.9O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 30.9O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 37.4O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 64.2O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 107.2O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 79.4O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 124.1O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 130.8O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 152.7O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 155.7O—C(O)—O—C(CH₃)₂—C═CH—CH₂—CH₂—O—C(O)—CH═CH, 171.2O—C(O)—O—C═CH—CH₂—CH₂—O—C(O)—CH₂—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17100 g/mol and 2.80.

EXAMPLE 7 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA⁵ (Monofunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G4, D4)

Example 1 is repeated, replacing, as chain-transfer agent, CTA¹ withCTA⁵ of formula:

A polymer is also recovered in liquid form, the ¹H NMR/¹³C NMR analysisof which gives the following values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=1.49 (s,O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 1.69 (d,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 2.25 (m,O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH—CH₂), 1.93 (m,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 4.20 (dd,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 5.31 and 5.61 (d,O—C(O)—O—C(═CH₂)—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 5.90 (m,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 7.02 (m,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=150.9O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH, 122.2O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH, 24.9O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—O(O)—CH═CH, 28.9O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—O(O)—CH═CH, 35.9O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 65.3O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—O(O)—CH═CH, 79.3O—C(O)—O—C(═CH₂)—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH, 122.2O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH), 150.9O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH, 152.7O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH, 161.6O—C(O)—O—C(═CH₂)—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH, 166.5O—C(O)—O—CH(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH═CH).

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formula:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17070 g/mol and 2.80.

EXAMPLE 8 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA⁶ (Difunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G4, D4)

Example 2 is repeated, replacing the CTA² with CTA⁶ of formula:

A polymer is also recovered in the form of a colourless liquid, in ayield of greater than 90%, the ¹H/¹³C NMR analysis of which gives thefollowing values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=1.49 (s,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 1.69 (d,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 1.93 (m,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 3.08O—C(O)—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 4.22 (dd,O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 5.44 (m,O—C(O)—O—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=24.9O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 28.9O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 35.9O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 37.4O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 65.3O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH), 79.3O—C(O)—O—C(═CH₂)—CH₂—C(CH₃)—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 124.1O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 130.8O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 152.7O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 161.6O—C(O)—O—C(═CH₂)—CH₂—C(CH₃)—CH₂—CH₂—O—C(O)—CH₂—CH═CH, 171.2O—C(O)—O—C(CH₃)—CH₂—CH₂—CH₂—O—C(O)—CH₂—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17120 g/mol and 2.80.

EXAMPLE 9 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA⁷(Monofunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G5, D5)

Example 1 is repeated, replacing, as chain-transfer agent, CTA¹ withCTA⁷ of formula:

A polymer is also recovered in liquid form, the ¹H NMR/¹³C NMR analysisof which gives the following values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=2.25 (m,O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH—CH₂), 2.31 (s,O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH), 4.73 (s,O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH), 5.87 (m,O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH), 7.08 (m,O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH).

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=10.5O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 62.8O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 144.3O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 150.9O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 122.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 122.2O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 153.0O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 155.7O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH, 166.5O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formula:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17050 g/mol and 2.80.

EXAMPLE 10 Depolymerization/Cyclization by Heating aPoly(Butadiene-Isoprene), Followed by Cross-Metathesis in the Presenceof CTA⁸ (Difunctional CTA Route) and Production of a Copolymer P SuchThat (G, D) is (G5, D5)

Example 2 is repeated, replacing the CTA² with CTA⁸ of formula:

A polymer is also recovered in the form of a colourless liquid, in ayield of greater than 90%, the ¹H/¹³C NMR analysis of which gives thefollowing values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=2.18O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 3.08O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 4.83O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 5.44O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH.

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit 20.0, 27.4,32.7, 37.4, 41.8, 124.2, 126.2, 131.4, end group=10.5O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 37.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 62.8O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 116.2O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 122.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 124.1O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 130.8O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 144.3O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 147.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 155.7O—C(O)—O—C(═C)—CH₂—O—C(O)—CH₂—CH═CH, 171.2O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH.

These values confirm that the product obtained is a copolymer comprisingtwo cyclocarbonate end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

and

-   -   of unit (II) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formulae:

The number-average molecular mass Mn and the polydispersity index are,respectively, 17080 g/mol and 2.80.

EXAMPLE 11 Depolymerization/Cyclization by HeatingPoly(Butadiene-Isoprene) in the Presence of Norbornene, Followed byCross-Metathesis in the Presence of CTA⁸

Example 10 is repeated, the 81.00 mmol of poly(butadiene-isoprene) beingreplaced in step (i) with a mixture of 41.00 mmol ofpoly(butadiene-isoprene) and of 40.00 mmol of norbornene, of formula:

available from the company Sigma-Aldrich.

The ratio r of the reagents, as defined previously, is equal to 0.27mmol divided by 41.00 mmol+40.00 mmol, i.e. 0.003.

After 8 hours, with effect from the addition of the CTA⁸, the productpresent in the flask is extracted after evaporation of the solvent undervacuum. The product is then recovered in a form that is liquid at roomtemperature, after precipitating from methanol, filtering and drying at23° C. under vacuum, in a yield of greater than 90%.

A polymer is also recovered in liquid form, the ¹H NMR/¹³C NMR analysisof which gives the following values:

¹H NMR (CDCl₃, 500 MHz, 298 K): δ (ppm) repeating unit 1.09 (s, CH₃isoprene unit), 2.06 and 2.11 (m, CH₂/isoprene and butadiene units),5.41 and 5.45 (m, CH═CH cis and trans/butadiene unit), 4.95 and 4.99 (m,CH═C(CH₃) cis and trans/isoprene unit), end group=2.18O—C(O)—O—C(CH₃)═C—CH₂O—C(O)—CH₂CH═CH, 3.08O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 4.83O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 5.50O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH—, 5.58O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH.

¹³C NMR (CDCl₃, 100 MHz, 298 K): δ (ppm) repeating unit: 27.4, 33.1,42.1, 43.4, 130.3, 133.1, end group=9.5O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 38.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 53.6O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 116.2O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 120.0O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 122.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 133.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 147.4O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH, 165.9O—C(O)—O—C(CH₃)═C—CH₂—O—C(O)—CH₂—CH═CH.

These values confirm that the polymer obtained is a copolymer comprisingtwo cyclocarbonate-like end groups, the main chain of which consistsessentially:

-   -   of unit (I) of formula:

-   -   of unit (II) of formula:

and

-   -   of unit (III) of formula:

and

of which two units (I) are each connected to one of the two end groupsof formula:

The number-average molecular mass Mn and the polydispersity index are,respectively, 22,450 g/mol and 2.80.

EXAMPLE 12 Synthesis of a Polyurethane Starting from the LiquidUnsaturated Polyolefin Bearing a Cyclocarbonate End Group of Example 2

The polyolefin of Example 2 was reacted at 80° C., in a stoichiometricratio, with a primary diamine of polyetherdiamine type (Jeffamine EDR176, Huntsman), until complete disappearance of the infrared bandcharacteristic of the (1,3-dioxolan-2-one-4-yl)methyl groups (at 1806cm⁻¹) and appearance of the bands characteristic of the carbamate bond(band at 1700 cm⁻¹).

The reaction time recorded for complete disappearance of the infraredband characteristic of the (1,3-dioxolan-2-one-4-yl)methyl groups wasabout 3 hours.

EXAMPLE 13 Synthesis of a Poly(Thio)Urethane Starting from the LiquidUnsaturated Polyolefin Bearing a Dithiocyclocarbonate End Group ofExample 4

The liquid unsaturated polyolefin bearing a dithiocyclocarbonate endgroup of Example 4 was reacted at 23° C., in a stoichiometric ratio,with a primary diamine of polyetherdiamine type (Jeffamine EDR 176,Huntsman), until total disappearance of the infrared band characteristicof the 2-thione-1,3-oxathiolan-4-yl groups (CS band at 1200 cm⁻¹ ininfrared) and appearance of the bands characteristic of thethiocarbamate bond (C═S band at 1530 cm⁻¹ in infrared) and of the thioland disulfide functions (SH band at 2500 cm⁻¹ and SS band at 510 cm⁻¹ inRaman).

The reaction time was about 3 hours.

EXAMPLE 14 Synthesis of a Polyurethane Starting from the LiquidUnsaturated Polyolefin Bearing a 2-oxo-1,3-dioxolen-4-yl End Group ofExample 10

The liquid unsaturated polyolefin bearing a 2-oxo-1,3-dioxolen-4-yl endgroup of Example 10 was reacted at 23° C., in a stoichiometric ratio,until total disappearance of the infrared band characteristic of the1,3-dioxolen-2-one groups (at 1800 cm⁻¹) and appearance of the bandscharacteristic of the 2-oxazolidinone groups (band between 1770 and 1780cm⁻¹) resulting from rapid post-cyclization of the keto-carbamatesobtained previously.

The reaction time was about 3 hours.

EXAMPLE 15 Synthesis of a Polyurethane Starting from the LiquidUnsaturated Polyolefin Bearing a 2-oxo-1,3-dioxolen-4-yl End Group ofExample 11

Example 14 is repeated, replacing the polyolefin of Example 10 with thepolyolefin bearing a 2-oxo-1,3-dioxolen-4-yl end group of Example 11.

The same result is obtained.

The invention claimed is:
 1. A hydrocarbon-based copolymer P comprisingtwo cyclocarbonate or dithiocyclocarbonate end groups F¹ and F² havingthe respective formulae:

in which: g and d, which may be identical or different, represent aninteger equal to 0, 1, 2 or 3; and G and D are two monovalent radicalssuch that the pair (G, D) is as follows: (G1, D1) of formulae:

in which A¹ is an alkylene group of 1 to 9 carbon atoms; (G2, D2) offormulae:

in which A² is an alkylene group of 1 to 9 carbon atoms; (G3, D3) offormulae:

in which: A³ is an alkylene group of 1 to 9 carbon atoms; A⁴, A⁵ and A⁶,which may be identical or different, each represent a hydrogen atom, alinear or branched alkyl radical of 1 to 6 carbon atoms, a cycloalkylradical of 5 or 6 carbon atoms, a phenyl radical or an alkylphenylgroup, the alkyl chain of which has 1 to 4 carbon atoms; (G4, D4) ofrespective formulae:

in which: A⁸ represents a hydrogen atom or a linear or branched alkylradical of 1 to 9 carbon atoms, A⁷ is an alkylene group of 1 to 9 carbonatoms or else a divalent radical of 1 to 20 carbon atoms and which maybe linear or branched, cyclic or heterocyclic with one or more oxygen orsulfur heteroatoms; (G5, D5) of respective formulae:

in which: A⁹ and A¹⁰, which may be identical or different, eachrepresent a hydrogen atom, a linear or branched alkyl radical of 1 to 6carbon atoms, a cycloalkyl radical of 5 or 6 carbon atoms, a phenylradical or an alkylphenyl group, the alkyl chain of which has 1 to 4carbon atoms; A⁹ and A¹⁰ also possibly being bonded together to form agroup —(CH₂—)_(q)— in which q is an integer ranging from 3 to 5; whereinthe main chain of said copolymer P comprises: a unit (I) of formula (I)repeated p times, p being an integer other than 0:

and a unit (II) of formula (II) repeated n times, n being an integerother than 0:

in which R⁰ represents a methyl radical or one of the three radicalshaving the following formula:

and, optionally, a unit (Ill) of formula (III) repeated m times, m beingan integer greater than or equal to 0:

in which: R¹, R², R³ and R⁴, which may be identical or different,represent: a hydrogen or halogen atom; or a radical of 1 to 22 carbonatoms which is alkyl, alkenyl, alkoxycarbonyl, alkenyloxycarbonyl,alkylcarbonyloxy, alkenylcarbonyloxy or alkylcarbonyloxyalkyl, thehydrocarbon-based chain of said radical possibly being optionallyinterrupted with at least one oxygen atom or one sulfur atom; inaddition: at least one of the groups R¹ to R⁴ can form, with at leastone other of the groups R¹ to R⁴ and with the carbon atom or atoms towhich said groups are linked, a 3- to 10-membered, optionallysubstituted, saturated or unsaturated hydrocarbon-based ring orheterocycle; and at least one of the pairs (R¹, R²) and (R³, R⁴) canform, with the carbon atom to which said pair is linked, a group of twocarbon atoms linked by a double bond: C═C, the other carbon atom ofwhich bears two substituents that are a hydrogen atom or a C₁-C₄ alkylradical; and the carbon atom bearing one of the groups of the pair (R¹,R²) may be linked to the carbon atom bearing one of the groups of thepair (R³, R⁴) by a double bond, it being understood that, in accordancewith the valency rules, only one of the groups of each of these twopairs is then present; R⁵ represents: an oxygen or sulfur atom, or adivalent radical —CH₂—, —C(═O)— or —NR⁶— in which R⁶ is an alkyl oralkenyl radical of 1 to 22 carbon atoms; it also being pointed out that:the bond

represents a single bond or a double bond; F¹ and F² are each linked toone of the two ends of the main chain and to a unit (I); and n, p and mare such that the number-average molecular mass Mn of the copolymer P iswithin a range extending from 400 to 100 000 g/mol and itspolydispersity index is within a range extending from 1.5 to 3.0.
 2. Thecopolymer P according to claim 1, wherein its main chain consistsessentially of the repeating unit (I) of formula (I), of the repeatingunit (II) of formula (II) and, optionally, of the repeating unit (III)of formula (III), and in that the number p of units (I) and the number nof units (II) are such that: p/(n+p) is between 45% and 95%, and n/(n+p)is between 5% and 55%.
 3. The copolymer P according to claim 1, whereinits main chain is such that: the unit (I) also has the formula (I′):

the unit (II) also has the formula (II′):

in which R⁰ represents a methyl radical or one of the three radicalshaving the following formula:

and, optionally, the unit (III) also has the formula (III′):

it being pointed out that, in the above formulae, the

bond is a single bond geometrically oriented on one side or the otherrelative to the double bond (cis or trans).
 4. The copolymer P accordingto claim 3, wherein its main chain is such that: on the p units offormula (I′), p″ also correspond to formula (I″), p″ being an integerother than 0, less than p and such that p″/p is greater than 0.8:

and on the n units of formula (II′), n″ also correspond to formula(II″), n″ being an integer other than 0, less than n and such that n″/nis greater than 0.9:


5. The copolymer P according to claim 1, wherein the radical R⁰ of theunit (II) represents a methyl radical.
 6. The copolymer P according toclaim 1, wherein F¹ and F² have the respective formulae:

in which: A¹ is a methylene group; and g and d are identical and equalto 0 or
 1. 7. The copolymer P according to claim 1, wherein F¹ and F²have the respective formulae:

in which: A² is a methylene group; and g and d are identical and equalto 0 or
 1. 8. The copolymer P according to claim 1, wherein F¹ and F²have the respective formulae:

in which: A³ is a —(CH₂)₂— group; A⁴ is a hydrogen atom; A⁵ and A⁶ areeach a methyl; and g and d are identical and equal to 0 or
 1. 9. Thecopolymer P according to claim 1, wherein F¹ and F² have the respectiveformulae:

in which: A⁷ is a propylene group; A⁸ is a methyl; and g and d areidentical and equal to 0 or
 1. 10. The copolymer P according to claim 1,wherein F¹ and F² have the respective formulae:

in which: A⁹ is a hydrogen atom; A¹⁰ is a methyl; and g and d areidentical and equal to 0 or
 1. 11. A process for preparing thehydrocarbon-based copolymer P as defined in claim 1, said processcomprising: (i) heating at a temperature ranging from 30° C. to 80° C.:(a) of a statistical bipolymer A chosen from a poly(butadiene-isoprene),a poly(butadiene-myrcene) and a poly(butadiene-farnesene); and (b)optionally in the presence of a compound B of formula (B):

and then (ii) heating the product formed in (i) to a temperature in arange from 20 to 60° C., in the presence of a chain-transfer agent (alsoreferred to as CTA), it being pointed out that: (c) when saidhydrocarbon-based copolymer P is such that the pair (G, D) is (G1, D1),(G3, D3), (G4, D4) or (G5, D5), then said CTA is a compound of formula(C1) or (C2):

in which: F¹ and F² are such that the pair (G, D) corresponds to thecorresponding definition (G1, D1), (G3, D3), (G4, D4) or (G5, D5); the

bond is a carbon-carbon single bond geometrically oriented on one sideor the other relative to the double bond (cis or trans); and (d) whensaid hydrocarbon-based copolymer P is such that the pair (G, D) is (G2,D2), then said CTA is the diepoxy compound of formula (C′1) or (C′2):

in which: F′¹e and F′²e are monovalent radicals of formulae (G′) and(D′):

the

bond is a carbon/carbon single bond geometrically oriented on one sideor the other relative to the double bond (cis or trans); it also beingpointed out that each of the steps (i) and (ii) is performed in thepresence of a metathesis catalyst and of a solvent; and then (iii) whensaid hydrocarbon-based copolymer P is such that the pair (G, D) is (G2,D2), a step of dithiocarbonation of the polymer obtained in step (ii),by reaction with carbon disulfide (CS₂) in the presence of a halogenatedlithium compound, at a temperature ranging from 10 to 45° C.
 12. Theprocess according to claim 11, wherein the bipolymer A used in (i) is apoly(butadiene-isoprene), preferably comprising from 45% to 95% bynumber of butadiene-based units and from 5% to 55% by number ofisoprene-based units, said percentages being expressed on the basis ofthe total number of constituent units of the poly(butadiene-isoprene)chain.
 13. The process according to claim 11, wherein the chain of thepoly(butadiene-isoprene) used in (i) comprises: less than 5% by numberof vinyl-1,2 butadiene units on the basis of the number ofbutadiene-based units, and less than 5% of the total number of vinyl-1,2isoprene units and of vinyl-3,4 isoprene units on the basis of thenumber of isoprene-based units.
 14. The process according to claim 11,wherein the chain of the poly(butadiene-isoprene) used in (i) comprises:at least 80% by number of cis-1,4 butadiene units on the basis of thenumber of butadiene-based units, and at least 90% by number of cis-1,4isoprene units on the basis of the number of isoprene-based units.
 15. Amixture functional as an adhesive comprising the hydrocarbon-basedpolymer as defined in claim 1 and an amine compound comprising at leasttwo amine groups.
 16. A process for assembling two substrates bybonding, comprising: coating at least one of the two substrates to beassembled with a liquid adhesive composition obtained by mixing an aminecompound comprising at least two amine groups with the hydrocarbon-basedpolymer as defined in claim 1; and then actually bringing the twosubstrates into contact.